The present invention relates to a method of separating HBr from hydrocarbons, especially from alkenes. This invention belongs to the field of chemical separation method of HBr from hydrocarbons.
The separation of HBr from hydrocarbons is seldom needed in the related field, so there are few related reports or patents. In our recent research, we designed a new process for conversion of methane or other lower hydrocarbons into higher hydrocarbon products, especially alkenes. For example, CN 200610031377.9 discloses a process as the following:
In the first step, namely reaction (A), low hydrocarbons, such as methane, react with HBr/H2O and oxygen over catalyst A to produce alkyl alkyl bromides, of which the reaction formula is shown below.
In the second step, namely reaction (B), alkyl bromides transform into high hydrocarbons such as alkenes, aromatics, and small alkanes, and HBr. The conversion of alkyl bromides can be higher than 99%. The reaction formula is shown below.
HBr will be produced in the reaction B. The HBr can be roughly washed using conventional methods, e.g. by feeding the HBr-containing hydrocarbons into the dilute HBr solution from reaction A to absorb the HBr. However, the certain amount of HBr remains in the products. Because of Lewis base property of alkenes, it is difficult to separate HBr from alkenes and aromatics completely by the conventional method.
The present invention discloses a purification method for HBr-containing hydrocarbons which comprise alkenes, aromatics and alkanes.
In the purification method, contacting the HBr-containing hydrocarbons with a silica supported metal oxide solid that is formulated as MOx/SiO2, where the metal oxide reacts with HBr to produce metal bromide. Then the metal bromide is oxidized by oxygen or oxygen of air to regenerate metal oxide on the support and the resultant Br2 is recycled at the same time.
In this process, HBr-containing hydrocarbons pass through a container filled with MOx/SiO2 and perform contacting by folwing through at a certain temperature (100˜600° C.). The metal oxide MOx reacts selectively with HBr to give non-volatile metal bromide and water to complete the purification of hydrocarbons. When the MOx/SiO2 reaches saturation absorbing HBr, the feedstock of HBr-containing hydrocarbons was switched to another container filled with MOx/SiO2 carrying out the same process.
The container filled with MOx/SiO2 absorbing HBr was purged by steam and then oxygen or air was fed into it to regenerate metal oxide at a certain temperature (250˜600 □) and recycle bromine simultaneously. Two or more coordinate containers filled with MOx/SiO2 operate purification-regeneration cycle to reach the purpose of purifying HBr-containing hydrocarbons and recovering bromine.
According to the present invention, MOx/SiO2 filled in the purification container is a silica supported compound selected from the group consisting of MgO, CoO, Co2O3, CuO and mixture thereof. The silica is commercial silica or prepared from silicon-containing precursor, such as silicates, SiCl4 or silica ester. The silica support was soaked in the solution comprising one or more soluble salts of acetate, nitrate and/or bromide of Mg, Co or Cu to give a mixture, then the mixture was dried and calcined to obtain the solid material of MOx/SiO2.
In the operation of absorbing HBr, when contacting the HBr of hydrocarbons and MOx/SiO2 the reaction between HBr and metal oxide MOx (MgO, CoO, Co2O3, CuO and mixture thereof) of MOx/SiO2 is carried out at a temperature of from about 100 □ to about 600 □, preferably from about 150 □ to about 400 □, more preferably from about 170 □ to about 300 □. After absorbing HBr, the step of regenerating MOx/SiO2 is carried out at a temperature of from about 250 □ to about 600 □, preferably from about 300 □ to about 500 □, more preferably between about 320 □ and about 450 □.
For performing the invention method to purifying the HBr-containing hydrocarbons, the system comprises 2˜8 MOx/SiO2 filled containers connected by switch valve. Every container filled with MOx/SiO2 can be a columnar fixed bed purification tower, which two ends are connected with switch valves. In a complete process, four steps of purifying, purging, regenerating and purging are carried out by switch valve. When the fixed bed purification tower is in the stage of absorbing, the inlet switch valve of purification tower is switched to HBr-containing hydrocarbons feedstock and the outlet switch valve of purification tower is switched to hydrocarbons tank. When the absorption of HBr reaches saturation, the hydrocarbons in the bed must be purged by steam and then oxygen could be fed into for regeneration. So the next step is purging stage. When the fixed bed purification tower is in the stage of purging, the inlet switch valve of purification tower is switched to the steam and the outlet switch valve of purification tower is switched to a gas-liquid separation tank, and the outlet of separation tank is connected to HBr-containing hydrocarbons. When the residual hydrocarbons is purged and the regeneration can be performed. In the stage of regenerating, the inlet switch valve of purification tower is switched to oxygen or air supplying system and the outlet switch valve of purification tower is switched to a Br2 storage tank. After regeneration, next operation can not be performed because there is some oxygen in the system. A purging process should be need to blow away the oxygen in the purification tower before next purification operation. In this operation the inlet switc valve of purification tower is switched to the steam and the outlet switch is switched to vent. On the operation process, the performing is not consecutive for every container, so at least two or more same purification tower are used to ensure consecutive purification of HBr-containing hydrocarbons. When a tower is in the stage of purifying, other towers are in the other three operating stages, so the complete process can be consecutively operated.
Preparation of metal oxide(s)/silica (MOx/SiO2)
Silica:
Silica can be commercial silica, or prepared from SiCl4 or silica ester. 120.0 mL of SiCl4 was added into 800 mL of water and stirred at ambient temperature for 12 h to get water-containing silica gel. Drying the water-containing silica gel at 120 □ for 6 h and calcining at 450 □ for 4 h to get silica. The silica was crushed and sieved to particles between 40 and 60 mesh.
The MOx/SiO2:
Adding 20.00 g of the silica particles and 99.25 mmol of dissoluble acetate, nitrate and/or bromide of M into 100 mL deionized water under stirring, impregnating at ambient temperature for 2 h and then drying at 120 □ for 6 h, finally calcining at 450 □ for 4 h to get the MOx/SiO2 which was then crushed and sieved to particles between 40 and 60 mesh.
The MOx in the MOx/SiO2 solid material was selected from the group consisting of MgO, CoO, Co2O3, CuO and their mixtures.
Purification of HBr-containing hydrocarbons:
A: propylene
B: methane (75%), isobutene (10.0%), propylene (1.0%), cyclopentene (6.0%), cyclohexane (3.0%), benzene (2.0%), toluene (1.0%) and xylene (2.0%).
Heating a quartz tube filled with quartz sand up to 200 □, pumping 40 wt % of HBr/H2O solution into the quartz tube at a rate of 3.0 mL/h, meanwhile A was directed into the quartz tube at a rate of 5.0 mL/min, the outlet of which was connected to a gas-liquid separation tank, to give a final outlet gas that is HBr-containing mixed gas. The outlet gas was introduced into AgNO3 solution (4.0 M, 5.0 mL) for determining the concentration of HBr in mixed gas. The concentration of HBr in mixed gas was 5.3 mol %.
The resultant mixed gas was directed into a reaction tube filled with 10.0 g of MgO/SiO2 solid material at 200 □, and the outlet gas from the reaction tube was introduced into AgNO3 solution(4.0 M, 5.0 mL) for determining the concentration of residual HBr. AgBr was produced when the MOx was exhausted. The volume of mixed gas was recorded at this time. The reaction tube was switched from HBr/C3H6 to steam and purged for 5 min. The solid material in the reaction tube was then regenerated by oxygen (or air) at 320˜450 □ until no bromine was flowed out, when the reaction tube was switched back to steam and purged for 5 min to complete a cycle process.
After three cycles, the system reached stable. Every gram of MgO/SiO2 can be applied for purification of 0.375 L of propylene that was equal to absorption of 0.1 g of HBr. The concentration of Br is 1.4×10−13 M when AgBr is appeared 7.0×10−16 mol of Br was contained in the 5.0 mL of AgNO3 solution (4.0M). These Br was arised from 3.75 L propylene, so the residual concentration of HBr in mixed gas was less than 1.87×10−16 mol/L.
The same result was obtained when purifying the mixture of B and HBr.
Number | Date | Country | Kind |
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200710034727.1 | Apr 2007 | CN | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/CN2008/000770 | 4/14/2008 | WO | 00 | 1/12/2010 |